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Calibration methods Chemistry 243. Figures of merit: Performance characteristics of instruments Precision Accuracy Selectivity Sensitivity Limit of Detection.

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Presentation on theme: "Calibration methods Chemistry 243. Figures of merit: Performance characteristics of instruments Precision Accuracy Selectivity Sensitivity Limit of Detection."— Presentation transcript:

1 Calibration methods Chemistry 243

2 Figures of merit: Performance characteristics of instruments Precision Accuracy Selectivity Sensitivity Limit of Detection Limit of Quantitation Dynamic Range

3 Precision vs. Accuracy in the common verbiage (Webster’s) Precision: The quality or state of being precise; exactness; accuracy; strict conformity to a rule or a standard; definiteness. Accuracy: The state of being accurate; exact conformity to truth, or to a rule or model; precision. These are not synonymous when describing instrumental measurements!

4 Precision and accuracy in this course Precision: Degree of mutual agreement among data obtained in the same way. Absolute and relative standard deviation, standard error of the mean, coefficient of variation, variance. Accuracy: Measure of closeness to accepted value Extends in between various methods of measuring the same value Absolute or relative error Not known for unknown samples Can be precise without being accurate!!! Precisely wrong!

5 Precision - Metrics Most important Often seen as % Handy, common

6 Sensitivity vs. Limit of Detection NOT THE SAME THING!!!!! Sensitivity: Ability to discriminate between small differences in analyte concentration at a particular concentration. calibration sensitivity—the slope of the calibration curve at the concentration of interest Limit of detection: Minimum concentration that can be detected at a known confidence limit Typically three times the standard deviation of the noise from the blank measurement (3s or 3  is equivalent to 99.7% confidence limit) Such a signal is very probably not merely noise

7 Calibration Curve, Limit of Detection, Sensitivity Signal 0 0 Analyte Mass or Concentration S/N = 3 Calibration Curve* LOD Sensitivity* = Slope *Same as Working Curve **Not improved by amplification alone

8 Selectivity Degree to which a method is free from interference from other contaminating signals in matrix No measurement is completely free of interferences Selectivity coefficient:

9 Calibration Curves: Sensitivity and LOD Signal 0 Analyte Mass or Concentration S/N = 3 LOD More Sensitive Less Sensitive LOD 0 For a given sample standard deviation, s, steeper calibration curve means better sensitivity Insensitive to amplification

10 Dynamic range The maximum range over which an accurate measurement can be made From limit of quantitation to limit of linearity LOQ: 10 s of blank LOL: 5% deviation from linear Ideally a few logs Absorbance: 1-2 MS, Fluorescence: 4-5 NMR: 6

11 Calibration Curves: Dynamic Range and Noise Regions Signal 0 0 Analyte Mass or Concentration S/N = 3 LOD Dynamic Range Calibration Curve Calibration Curve becomes poor above this amount of analyte Noise Region LOQ Poor Quant LOL

12 Types of Errors Random or indeterminate errors Handled with statistical probability as already shown Systematic errors Instrumental errors Personal errors Method errors Gross errors Human error Careless mistake, or mistake in understanding Often seen as an outlier in the statistical distribution “Exactly backwards” error quite common

13 Systematic errors Present in all measurements made in the same way and introduce bias. Instrumental errors Wacky instrument behavior, bad calibrations, poor conditions for use Electronic drift, temperature effects, 60Hz line noise, batteries dying, problems with calibration equipment. Personal errors Originate from judgment calls Reading a scale or graduated pipette, titration end points Method errors Non-ideal chemical or physical behavior Evaporation, adsorption to surfaces, reagent degradation, chemical interferences

14 Instrument calibration Determine the relationship between response and concentration Calibration curve or working curve Calibration methods typically involve standards Comparison techniques External standard* Standard addition* Internal standard* * calibration curve is required

15 External standard calibration (ideal) External Standard – standards are not in the sample and are run separately Generate calibration curve (like PS1, #1) Run known standards and measure signals Plot vs. known standard amount (conc., mass, or mol) Linear regression via least squares analysis Compare response of sample unknown and solve for unknown concentration All well and good if the standards are just like the sample unknown

16 Signal 0 0 Analyte Mass or Concentration S/N = 3 LOD External standard calibration (ideal) Sample Unknown Sample Unknown Amount External Calibration Standards including a blank

17 In class example of external standard calibration Skoog, Fig Signal 0 0 Analyte Mass or Concentration S/N = 3 LOD Sample Unknown Sample Unknown Amount External Calibration Standards including a blank

18 Real-life calibration Subject to matrix interferences Matrix = what the real sample is in pH, salts, contaminants, particulates Glucose in blood, oil in shrimp Concomitant species in real sample lead to different detector or sensor responses for standards at same concentration or mass (or moles) Several clever schemes are typically employed to solve real-world calibration problems: Internal Standard Standard Additions

19 Internal standard A substance different from the analyte added in a constant amount to all samples, blanks, and standards or a major component of a sample at sufficiently high concentration so that it can be assumed to be constant. Plotting the ratio of analyte to internal-standard as a function of analyte concentration gives the calibration curve. Accounts for random and systematic errors. Difficult to apply because of challenges associated with identifying and introducing an appropriate internal standard substance. Similar but not identical; can’t be present in sample Lithium good for sodium and potassium in blood; not in blood

20 Standard additions Classic method for reducing (or simply accommodating) matrix effects Especially for complex samples; biosamples Often the only way to do it right You spike the sample by adding known amounts of standard solution to the sample Have to know your analyte in advance Assumes that matrix is nearly identical after standard addition (you add a small amount of standard to the actual sample) As with “Internal Standard” this approach accounts for random and systematic errors; more widely applicable Must have a linear calibration curve

21 How to use standard additions To multiple sample volumes of an unknown, different volumes of a standard are added and diluted to the same volume. Fixed parameters: c s = Conc. of std. – fixed V t = Total volume – fixed V x = Volume of unk. – fixed c x = Conc. of unk. - seeking Non-Fixed Parameter: V s = Volume of std. – variable Calibration Standard (Fixed c s ) VxVx VxVx VxVx VxVx V s3 V s2 V s4 V s1 VtVt VtVt VtVt VtVt Volume top-off step: V x diluted to V t V s diluted to V t

22 How to use standard additions To multiple sample volumes of an unknown, different volumes of a standard are added and diluted to the same volume. Combined Signal Concentration 0 0 S1S1 S2S2 S4S4 S3S3

23 How to use standard additions 0 0 Concentration Combined Signal k = slope or sensitivity

24 How to use standard additions Signal from standard Signal from unknown

25 How to use standard additions Remember, V std is the variable. Knowns: c std V total V x

26 How to use standard additions 0 0 VsVs S, Combined Signal Get m (slope) and b (intercept) from linear least squares How do I handle k ?

27 Determine c x via standard curve extrapolation … At the x-intercept, S = 0 Seeking [analyte] known Skoog, Fig V std when S = 0

28 … or determine c x by directly using fit parameters Final calculation: All knowns … in conclusion, an easy procedure to perform and interpret; you take values you know and do a linear least squares fit to get m and b


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